0 5212Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple1China (ByteDance, Huawei, Baidu…)0Others2Total5Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 8,744 East Asian ancestry individuals; replicated in 19,041 East Asian ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.153 higher; p = 2 × 10−12.
How common The G allele had a frequency of about 18% in the people studied.
Where it sits Chromosome 1, band 1p32.3 — in an intron of MAGOH.
What each result means
G/GTwo copies of the version the research linked to Neonatal adipoylcarnitine (C6DC) levels (maternal genotype effect). That is the strongest link of the three results. A link in a study is not a diagnosis.
G/TOne copy of the version the research linked to Neonatal adipoylcarnitine (C6DC) levels (maternal genotype effect). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Neonatal adipoylcarnitine (C6DC) levels (maternal genotype effect). This is the starting point the study compared everyone against.
Cell genomics · 2024 · PMID 39389019 · open access
Questions about rs12082305
What is rs12082305?
rs12082305 is a single position in the genome, in or near the MAGOH gene. Published research associates it with neonatal adipoylcarnitine (c6dc) levels (maternal genotype effect). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs12082305 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs12082305 come from?
GWAS Catalog, Cell genomics 2024, PMID:39389019. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 5212Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple1China (ByteDance, Huawei, Baidu…)0Others2Total5Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.